NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES— 510(k) K983597

Name: FDA 510(k) clearance K983597
Creator: U.S. Food and Drug Administration
Published: 1999-01-11

Substantially Equivalent

Medicotest, Inc.

FDA 510(k) clearance K983597 for NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES, Substantially Equivalent on 1999-01-11. Applicant: Medicotest, Inc.. Device class: 2.

Clearance details

Applicant: Medicotest, Inc.
Product code: Code GXZ
Device class: Class 2
Regulation: 21 CFR 882.1350
Advisory panel: Neurology
Date received: 1998-10-13
Decision date: 1999-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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